Product Recalls in Oregon
Product recalls affecting Oregon — including food, drugs, consumer products, medical devices, and vehicles distributed to Oregon. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,457 recalls have been distributed to Oregon in the last 12 months.
Showing 28141–28160 of 28,488 recalls
Recalled Item: Plum A+ Hyperbaric Infusion Pump Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+3 Infusion Pump System Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "****ORTHO SENSOR**12-123-A Knee Trial for Trithion***1560 Saw grass...
The Issue: Ortho sensor in Sunrise, FL is recalling the Graphics User Interface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBAS AmpliPrep Sample Tube Input Barcode Clips Recalled by Roche Molecular...
The Issue: Certain lots of COBAS AmpliPrep (CAP) S-tube Input (Box of 12 bags 12x24...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMAGE Immunochemistry Systems Rheumatoid Factor (RF) Reagent Recalled by...
The Issue: The recall was initiated because Beckman Coulter has confirmed customer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker T2 Arthrodesis Nailing System. Manufacturer: Stryker Trauma GmbH...
The Issue: Stryker has become aware that there exists a potential for breach of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 20mm Recalled by Exactech, Inc. Due to...
The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 40mm Recalled by Exactech, Inc. Due to...
The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 40mm Recalled by Exactech, Inc. Due to...
The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 30mm Recalled by Exactech, Inc. Due to...
The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 30mm Recalled by Exactech, Inc. Due to...
The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 20mm Recalled by Exactech, Inc. Due to...
The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VMX Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware of...
The Issue: GE Healthcare has become aware of an issue associated with the base casting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER PrepPlus Recalled by Beckman Coulter Inc. Due to The recall was...
The Issue: The recall was initiated because Beckman Coulter has confirmed that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEE-1000A Neuromaster Recalled by Nihon Kohden America Inc Due to The...
The Issue: The MEE-1000A Neuromaster had defective printed circuit boards (PCBs). Gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker AVS Navigator Trials 6mm-15mm Manufactured by: Stryker Spine SAS...
The Issue: Beginning in February 2011, Stryker Spine began receiving reports related to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.